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HRID 67228作成日:2026年10月25日

Triethylamine → 2-(o-Chlorophenyl)-3-(3,4-dimethoxyphenyl)-2,3,5,6,7,8-hexahydrothiazolo[3,2-a][1,3]diazepin-3-ol

https://huagongshe.com/reaction/67228

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物1,3-Diazepane-2-thioneHCID 736589—
反応物2-(2-Chlorophenyl)-1-(3,4-dimethoxyphenyl)-2-hydroxyethan-1-oneHCID 15044219—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物2-(o-Chlorophenyl)-3-(3,4-dimethoxyphenyl)-2,3,5,6,7,8-hexahydrothiazolo[3,2-a][1,3]diazepin-3-olHCID 13068287—

反応手順

A 6.13 g. portion of 2'-chloro-3,4-dimethoxybenzoin, 5.6 ml. of triethylamine and 20 ml. of toluene are mixed and stirred. A mixture of 1.55 ml. of methanesulfonyl chloride in 40 ml. of toluene is added over a period of one hour. A 50 ml. portion of water and more toluene are added. The organic layer is separated, washed with water and concentrated in vacuo to give 8.3 g. of 2'-chloro-3,4-dimethoxybenzoin methanesulfonate ester as a viscous oil. A mixture of this oil in 30 ml. of acetone is added to a stirred mixture of 1.95 g. of hexahydro-2H-1,3-diazepine-2-Thione in 150 ml. of acetone. The resulting mixture is stirred for 3 hours, then 3 hours at 45°-50° C., concentrated to 1/3 of its original volume and ether is added producing a gum. The mixture is concentrated free of solvents, 100 ml. of water and 2 ml. of ammonium hydroxide are added and the solid is filtered and washed with water. This solid is dissolved in 20 ml. of ethanol and refrigerated giving 1.3 g. of the desired product, m.p. 98°-100° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04344954
出典データセットuspto-grants-1982_08
ORD IDord-3dd7ab568a7044628a6fc2869f0d7c63
出典メモuspto-grants-1982_08